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- W2095987120 abstract "However, these methods cannot begeneralized as much as is desirable, and they yielded poorchemo- and/or stereoselectivities. Hence, the developmentof an efficient enantioselective synthetic method for obtain-ing 2,3-dihydrobenzofuran scaffolds attracted our attention.As part of the research program related to the developmentof synthetic methods for the enantioselective construction ofstereogenic carbon centers, we recently developed a novelcatalytic asymmetric 1,4-addition reaction of o-hydroxy-cinnamaldehydes using organocatalyst, which affordedenantio-enriched chroman derivatives." @default.
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- W2095987120 date "2012-08-20" @default.
- W2095987120 modified "2023-10-16" @default.
- W2095987120 title "One-Pot Cascade Michael-Cyclization Reactions of o-Hydroxycinnamaldehydes: Synthesis of Functionalized 2,3-Dihydrobenzofuranes" @default.
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- W2095987120 doi "https://doi.org/10.5012/bkcs.2012.33.8.2781" @default.
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